Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.46 (A)
Location

Chromosome 18:22987010 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58051785, rs56514252

This variation has 8 HGVS names - click the plus to show

18:g.22987010C>A
ENST00000399722.3:c.709+2020C>A
ENST00000399721.3:c.709+2020C>A
ENST00000585177.1:c.*282+2020C>A
ENST00000360790.6:c.709+2020C>A
ENST00000577445.1:c.425+2020C>A
ENST00000399725.3:c.709+2020C>A
ENST00000327155.6:c.709+2020C>A

This variation has assays on 8 chips - click the plus to show

Variation displays